HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ciprofloxacin → HCID 13850789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ciprofloxacin | HCID 2764 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chloromethyl trifluoromethyl sulfide | HCID 3468030 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13850789 | HCID 13850789 | 33.7% |
Reaction Steps
3.3 g (10 mmol) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid are heated at 90° in 50 ml of dimethylformamide with 4 g (27 mmol) of trifluoromethylthiomethyl chloride, 2.1 g of triethylamine, 1.7 g of potassium iodide and 0.2 g of tetrabutylammonium iodide for 16 hours. The solution is poured into 50 ml of water and the precipitate is filtered off with suction and boiled up with methanol. 1.5 g of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-trifluoromethylthiomethyl-1-piperazinyl)-3-quinolinecarboxylic acid of melting point 247°-250° (with decomposition) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04806539 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-dd39ef5f55064a55989d36b24fe33c2d |
| Source note | uspto-grants-1989_02 |